However, there have been reports of Dravet syndrome caused by SCN1A variants inherited from mildly affected parents, as well as some individuals with de novo loss-of-function or premature truncation variants that presented with milder phenotypes, like generalized epilepsy with febrile seizures plus (GEFS+) (Depienne et al. 2010, 2009; Goldberg-Stern et al. 2014; Guerrini et al. 2010; Nabbout et al. 2003; Osaka et al. 2007; Yordanova et al. 2011; Yu et al. 2010). Here, SCN1A is linked to Dravet syndrome.